FDA UDI In Commercial Distribution 🇺🇸 United States

Mio Advance

DI: 05705244016262 · Model: MMT-232 · Unomedical A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Mio Advance
Primary DI
05705244016262
Version / Model
MMT-232
Company Name
Unomedical A/S
Labeler DUNS
306032491
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2018-04-15
Public Version
3
Public Version Date
2023-09-25
Public Version Status
Update
Public Device Record Key
f15e7c0b-b95e-459d-94ee-4fc296622c9c

Device Description

Single use infusion set for subcutaneous infusion. The infusion set must be used as described in the Instruction for Use.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
35833 Electric infusion pump administration set, single-use

Identifiers

Type ID
Package 05705244016279
Primary 05705244016262
Unit of Use 05705244016286

Customer Contacts

Device Sizes

Type Value Unit Text
Length 60 Centimeter
Depth 6 Millimeter
Angle 90 degree

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store infusion sets in a cool, dry location at room temperature. Do not store infusion sets in direct sunlight. Do not store infusion sets where it is humid.